| Product NDC: | 10096-0206 |
| Proprietary Name: | Solutions |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
| Active Ingredient(s): | 20; 75; 30; 30 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10096-0206 |
| Labeler Name: | Avon Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100607 |
| Package NDC: | 10096-0206-1 |
| Package Description: | 100 mL in 1 BOTTLE, PUMP (10096-0206-1) |
| NDC Code | 10096-0206-1 |
| Proprietary Name | Solutions |
| Package Description | 100 mL in 1 BOTTLE, PUMP (10096-0206-1) |
| Product NDC | 10096-0206 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100607 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Avon Products, Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 20; 75; 30; 30 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |